Clinical Trials Logo

Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03229421
Other study ID # STU00205325
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date July 6, 2017
Est. completion date December 31, 2018

Study information

Verified date January 2019
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether any diagnostic patterns exist in the symptom presentation of Zika Virus.


Description:

The study has both retrospective and prospective components. The retrospective review includes medical records with laboratory confirmed Zika Virus diagnosis and the prospective component will enroll adults presenting with febrile illness and rash and ask them to complete a survey about their symptoms. Diagnostic testing will be completed to confirm infection source.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults aged 18 years and older presenting with febrile illness and rash

Exclusion Criteria:

- Patients aged 17 years or younger

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Survey
18 question symptom assessment tool including non-identifying demographic information questions.

Locations

Country Name City State
Dominican Republic Pontificia Universidad Catolica Madre y Maestra, Departamento de Medicina Santo Domingo Illinois

Sponsors (2)

Lead Sponsor Collaborator
Northwestern University Pontificia Universidad Catolica Madre y Maestra

Country where clinical trial is conducted

Dominican Republic, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of days with specific symptoms Number of days reported experiencing specific symptoms due to Zika Virus infection and and associated characteristics such as location and intensity 20 minutes
Secondary Frequency measures of initial clinical presentations Frequency of reported symptoms at initial clinical presentation. 20 minutes